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1.
Infect Immun ; 69(6): 3744-54, 2001 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-11349039

RESUMEN

The Staphylococcus aureus genome encodes three ferric uptake regulator (Fur) homologues: Fur, PerR, and Zur. To determine the exact role of PerR, we inactivated the gene by allelic replacement using a kanamycin cassette, creating strain MJH001 (perR). PerR was found to control transcription of the genes encoding the oxidative stress resistance proteins catalase (KatA), alkyl hydroperoxide reductase (AhpCF), bacterioferritin comigratory protein (Bcp), and thioredoxin reductase (TrxB). Furthermore, PerR regulates transcription of the genes encoding the iron storage proteins ferritin (Ftn) and the ferritin-like Dps homologue, MrgA. Transcription of perR was autoregulated, and PerR repressed transcription of the iron homeostasis regulator Fur, which is a positive regulator of catalase expression. PerR functions as a manganese-dependent, transcriptional repressor of the identified regulon. Elevated iron concentrations produced induction of the PerR regulon. PerR may act as a peroxide sensor, since addition of external hydrogen peroxide to 8325-4 (wild type) resulted in increased transcription of most of the PerR regulon, except for fur and perR itself. The PerR-regulated katA gene encodes the sole catalase of S. aureus, which is an important starvation survival determinant but is surprisingly not required for pathogenicity in a murine skin abscess model of infection. In contrast, PerR is not necessary for starvation survival but is required for full virulence (P < 0.005) in this model of infection. PerR of S. aureus may act as a redox sentinel protein during infection, analogous to the in vitro activities of OxyR and PerR of Escherichia coli and Bacillus subtilis, respectively. However, it differs in its response to the metal balance within the cell and has the added capability of regulating iron uptake and storage.


Asunto(s)
Proteínas Bacterianas , Regulación Bacteriana de la Expresión Génica , Hierro/metabolismo , Estrés Oxidativo/fisiología , Proteínas Represoras , Staphylococcus aureus/patogenicidad , Factores de Transcripción , Secuencia de Aminoácidos , Animales , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Secuencia de Bases , Catalasa/genética , Catalasa/metabolismo , Farmacorresistencia Microbiana , Humanos , Peróxido de Hidrógeno/farmacología , Ratones , Datos de Secuencia Molecular , Proteínas Represoras/genética , Proteínas Represoras/metabolismo , Infecciones Estafilocócicas/microbiología , Infecciones Estafilocócicas/fisiopatología , Staphylococcus aureus/fisiología , Transcripción Genética , Virulencia
7.
MSDA J ; 39(2): 85-6, 1996.
Artículo en Inglés | MEDLINE | ID: mdl-9569880

RESUMEN

To identify chemically dependent patients, dentists should explore whether the patients have any history of, or are recovering from, chemical dependency. Occasionally, dental treatment plans must be modified for active or recovering chemically dependent patients. Dentists need to be alert for chemically dependent patients who are doctor-shopping and present themselves to dentists to secure narcotic analgesics. Dentists should be aware that chemical dependency is a disease, and the management of chemically dependent patients may require certain adjustments.


Asunto(s)
Atención Dental para Enfermos Crónicos/métodos , Relaciones Dentista-Paciente , Trastornos Relacionados con Sustancias/rehabilitación , Humanos , Planificación de Atención al Paciente , Trastornos Relacionados con Sustancias/diagnóstico
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